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Lutidinic acid

From Wikipedia, the free encyclopedia
Lutidinic acid
Names
Preferred IUPAC name
Pyridine-2,4-dicarboxylic acid
Other names
2,4-Pyridinedicarboxylic acid
Identifiers
3D model (JSmol)
131631
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.007.176 Edit this at Wikidata
EC Number
  • 207-892-2
279731
UNII
  • InChI=1S/C7H5NO4/c9-6(10)4-1-2-8-5(3-4)7(11)12/h1-3H,(H,9,10)(H,11,12)
    Key: MJIVRKPEXXHNJT-UHFFFAOYSA-N
  • O=C(O)c(c0)nccc0C(O)=O
Properties
C7H5NO4
Molar mass 167.120 g·mol−1
Melting point 242–243 °C (468–469 °F; 515–516 K)[1]
Hazards
GHS labelling:
GHS07: Exclamation mark
Warning
H315, H319, H335
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Lutidinic acid (pyridine-2,4-dicarboxylic acid) is an heterocyclic organic compound, more precisely a heteroaromatic. It belongs to the group of pyridine dicarboxylic acids and consists of a pyridine ring which carries two carboxy groups in the 2- and 4-position.[2][3]

References

[edit]
  1. ^ "Safety Data Sheet" (in German).
  2. ^ Meyer, Hans; Tropsch, Hans (1914). "Über Derivate der Lutidinsäure und das αγ-Diaminopyridin". Monatshefte für Chemie. 35 (2): 189–206. doi:10.1007/BF01518123. S2CID 104461279.
  3. ^ Richard Wolffenstein: Die Pflanzenalkaloide, 3. Auflage, Berlin 1922, S. 67 ([1], p. 67, at Google Books)